Last Updated: November 13, 2026

Details for New Drug Application (NDA): 070752

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NDA 070752 describes NALBUPHINE, which is a drug marketed by Abraxis Pharm, Abbvie, Abbott, Dr Reddys, Hospira, Igi Labs Inc, Rising, and Somerset Theraps Llc, and is included in nineteen NDAs. Additional details are available on the NALBUPHINE profile page.

The generic ingredient in NALBUPHINE is nalbuphine hydrochloride. There is one drug master file entry for this compound. Six suppliers are listed for this compound. Additional details are available on the nalbuphine hydrochloride profile page.

Summary for 070752

Tradename:	NALBUPHINE
Applicant:	Abraxis Pharm
Ingredient:	nalbuphine hydrochloride
Patents:	0

Medical Subject Heading (MeSH) Categories for 070752

Analgesics, Opioid
Narcotic Antagonists
Narcotics

Profile for product number 001

Active Rx/OTC/Discontinued:	DISCN	Dosage:	SOLUTION;INTRAMUSCULAR, INTRAVENOUS, SUBCUTANEOUS			Strength	20MG/ML (20MG/ML)
Approval Date:	Sep 24, 1986	TE:		RLD:	No

Profile for product number 002

Active Rx/OTC/Discontinued:	DISCN	Dosage:	SOLUTION;INTRAMUSCULAR, INTRAVENOUS, SUBCUTANEOUS			Strength	200MG/10ML (20MG/ML)
Approval Date:	Sep 24, 1986	TE:		RLD:	No

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